On February 3,, Biomet and attorneys representing the many plaintiffs in defective hip lawsuits agreed to a settlement, which federal Judge Robert Miller, Jr. Attorneeys leading national Zimmer Biomet Holdings ( ZBH) hip litigation. Anyone who underwent shoulder replacement or implant surgery from through December of and received a Zimmer Biomet implant should learn if their device is included. District Court for the North District of Indiana before the Honorable Robert L. Biomet lawsuit update. Food and Drug Administration received hundreds of reports of these sorts of complications from doctors and patients who used the implant.
The Zimmer Biomet Shoulder Recall affects implants distributed between October and September, which could have been used in implants up to the date of the recall. Dec 08, · The M2a Magnum was a metal- on- metal hip design. This order requires that all pending and future Biomet M2a Magnum hip lawsuits be transferred to the U.
The Indiana- based medical device company Biomet, which merged with another device maker Zimmer in to form Zimmer Biomet, has faced hundreds of lawsuits over its Biomet M2a Magnum and Biomet M2a38 metal- on- metal hip replacement systems. You may have a Biomet M2a Metal on Metal Hip Lawsuit. S District Court for the Northern District of Indiana – assigned to oversee the coordinated multidistrict cases – subsequently approved. What Problems Have Been Linked to the Biomet Hip? Biomet M2a Magnum and M2a38. According to lawsuits, the metal parts wore against each other and released microscopic metal ions, which caused a wide variety of complications, including metallosis. As of February, at least 1, 141 Biomet hip implant lawsuits had been filed.